Amino Acids (AA)

<p>Prolintane hydrochloride is a drug that has been shown to inhibit the activity of enzymes in the inflammatory and immune responses. It also inhibits the uptake of caffeine, which may be due to its ability to bind with the toll-like receptor (TLR) and CB2 receptor. Prolintane hydrochloride has been used to treat bowel disease, depression, and autoimmune diseases such as rheumatoid arthritis. This drug has a depressant effect on the central nervous system, which may lead to symptoms such as drowsiness and fatigue. The drug is metabolized through a synthetic pathway that involves N-deacetylation by acetyltransferase enzymes. Prolintane hydrochloride also inhibits inflammatory bowel disease by reducing cytokine production in mice with colitis.</p>

<p>5-Fluoro-2-methylphenylhydrazine hydrochloride is a crystalline solid that is soluble in water. It is used as a reagent in organic synthesis, but it also has application as an intermediate in the production of calcium hydroxide and calcium fluoride. 5-Fluoro-2-methylphenylhydrazine hydrochloride reacts with methacrylate to produce an ultrafine powder, which can be difficult to hydrate because of its high molecular weight. The hydration reaction requires the addition of large amounts of water and heat. This process can be accelerated by adding a solution of calcium ions or calcium hydroxide to the reaction mixture. Hydrogen fluoride gas (HF) may also be generated during this process. Crystallization occurs when the solids are heated or placed in contact with a nonpolar solvent such as hexane.</p>

<p>2-Fluoro-3-methylbenzoic acid methyl ester is a small molecule that has been shown to possess 5-HT3 receptor antagonist activity in the range of nanomolar potencies. This drug has also been shown to be orally active in mice. The physicochemical properties of 2-fluoro-3-methylbenzoic acid methyl ester include a melting point of 155.5° C, solubility in methanol and acetone, and a molecular weight of 168.2 g/mol.<br>2-Fluoro-3-methylbenzoic acid methyl ester is being developed as a targeted agent for the treatment of bowel syndrome, which is characterized by abdominal pain, nausea and diarrhea.</p>

<p>2-Phenoxybenzaldehyde is an organic compound that belongs to the heterocyclic aldehyde family. It is a white solid with a strong, pleasant odor. 2-Phenoxybenzaldehyde is used as an intermediate in organic synthesis, and has been shown to inhibit the receptor activity of human leukocyte antigen (HLA) class II molecules. The reaction mechanism for this inhibition is not known. The reaction of 2-phenoxybenzaldehyde with hydrochloric acid produces phenylhydroxylamine, which can be oxidized by inorganic acids to form phenyloxalic acid. This compound also inhibits the production of inflammatory cytokines such as TNFα and IL-1β in vitro and in vivo.</p>

<p>7-Diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin is a fluorescent probe that can be used to measure the cytosolic calcium concentration. This probe binds to heparin, which is a positive ionic charge and has been shown to cause an increase in cytosolic calcium levels in cultured cells. 7-Diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin has been used to successfully monitor changes in cytosolic calcium levels in response to pharmacological agents, such as the monoclonal antibody TNF-α. 7-Diethylamino-3-(4'-maleimidylphenyl)-4-methylcoumarin has also been used as a marker for tissue culture studies, where it was found that this molecule binds to the ryanodine receptor and alters its redox potential.</p>

2-Methylnicotinic acid imidazolide is a small molecule with the ability to regulate RNA splicing. It has been shown to inhibit the transcription of specific genes by binding to the RNA sequence and forming a stable complex with the mRNA. The chemical structure of 2-methylnicotinic acid imidazolide has also been shown to be similar to that of nicotinamide, which is a precursor for NAD+, a coenzyme involved in cellular metabolism. This may explain how 2-methylnicotinic acid imidazolide regulates gene expression and promotes neuronal health.

<p>L-Cysteine is a non-essential amino acid that is used in biochemical research and has been shown to inhibit the activity of nicotinic acetylcholine receptors. It also regulates the response of cells to toll-like receptor ligands by inhibiting the production of inflammatory mediators. L-Cysteine binds to a sequence called response element, which is found in many prokaryotic genes, and inhibits protein oxidation. L-Cysteine has an inhibitory effect on single-stranded RNA and can act as a rate constant for protein synthesis. L-Cysteine is an amino acid that contains sulfur and can be found in proteins with thiol groups. The cysteine residues in proteins are coordinated geometrically by a zinc ion (Zn2+) or iron ion (Fe3+). This coordination geometry affects the biological properties of these proteins.</p>

<p>O-tert-Butyl-D-serine t-butyl ester hydrochloride is a reaction component that can be used as a reagent in research and chemical synthesis. This compound is useful for the synthesis of complex compounds, such as pharmaceuticals and agrochemicals. It is also used in the production of fine chemicals, such as dyes and perfumes. CAS No. 179559-35-4</p>

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<p>Fmoc-N-methyl-L-isoleucine is a high quality reagent that is used as an intermediate for the synthesis of complex compounds. It is a useful building block for the synthesis of speciality chemicals and research chemicals. Fmoc-N-methyl-L-isoleucine is also a versatile building block that can be used in reactions involving nucleophilic substitution, reductive amination, Mannich reaction, and hydrogenation. This chemical has been shown to have antihypoxic effects on neurons in vitro.</p>

<p>H-Leu-Asp-OH is a phenolic compound that is synthesized by the esterification of L-leucine and L-aspartic acid. The solubility of H-Leu-Asp-OH in organic solvents, such as dichloromethane and ethanol, is higher than in water. This product can be used as a solvent for other substances and as a boosting agent for other products during clinical trials. It has been shown to have health effects on humans, but more research is needed to determine any possible side effects or long term health problems.</p>

<p>5-Methoxy-3-methylbenzonitrile is a versatile chemical with a wide range of applications in pharmaceuticals, agrochemicals, and other industries. It is used as a reaction component in the synthesis of drugs such as indomethacin and methotrexate. It is also useful for the production of high-quality research chemicals. 5-Methoxy-3-methylbenzonitrile has been shown to be an efficient building block for the synthesis of complex compounds with diverse structures.</p>

<p>2,6-Di-tert-butyl-4-methylpyridine (2,6-DBMP) is a thianthrene derivative that has been used in asymmetric synthesis and transfer reactions. 2,6-DBMP is synthesized by reacting the appropriate carbonyl chloride with the corresponding 2,6-di-tert butylpyridine. It can also be prepared by the palladium catalyzed coupling of a benzyl halide and an allyl bromide. The compound's stereoselectivity depends on the reactants' configuration at C2. This property makes it useful for the preparation of chiral molecule such as oligosaccharides and methyl glycosides. 2,6-DBMP has shown to have immunomodulatory activity against mutant strains of human erythrocytes in vitro.</p>

<p>2,4-Dioxo-4-phenylbutanoic acid is an inhibitor of the influenza virus that binds to its surface proteins and inhibits the replication of the virus. 2,4-Dioxo-4-phenylbutanoic acid is a stable complex that has been shown to be active against HIV. This compound has been shown to inhibit viral life by binding to the subunits of influenza A and B viruses. 2,4-Dioxo-4-phenylbutanoic acid has been synthesized as an active analogue of zanamivir and it is believed that this compound binds to the same site on the influenza A virus as zanamivir. The molecule is also tautomerizable, which means it can exist in two forms: ketone (the more stable form) or enol (less stable).</p>

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<p>4-Bromo-2-methylbenzoic acid ethyl ester is a high quality and versatile building block. It is a useful intermediate in the synthesis of organic compounds, and can be used as a reaction component in the synthesis of complex compounds. 4-Bromo-2-methylbenzoic acid ethyl ester is also a useful scaffold for the construction of new chemical entities. It has been shown to react with potassium tert-butoxide to produce 4-(2,6-dimethylphenyl)piperidine (CAS No. 220389-34-4).</p>

<p>1-Linoleoyl-rac-glycerol is a lipid with a structure similar to that of linoleic acid. The compound is used as a substrate for the study of the effects of oxygenation on lipid metabolism. 1-Linoleoyl-rac-glycerol has been shown to have anti-inflammatory properties in chronic kidney disease and pancreatitis models, which may be due to its inhibition of pancreatic lipase. 1-Linoleoyl-rac-glycerol is also used as a reaction product in sample preparation techniques, such as thin layer chromatography and high performance liquid chromatography. A variety of reactions can be performed with this compound, including hydrolysis by thrombin or trypsin, esterification with methanol or chloroform, or oxidation by potassium permanganate. 1-Linoleoyl-rac-glycerol has been shown to inhibit the growth of human lung epithelial cells (thp1</p>

<p>N-(2-Chlorobenzyl)-1-phenylpropan-2-amine hydrochloride (CBP) is a potent stimulant drug that is used to treat chronic pain. It has been shown to be effective in the treatment of alopecia areata and inflammatory diseases, such as Crohn's disease, ulcerative colitis, and rheumatoid arthritis. CBP blocks protein synthesis by inhibiting the activity of the enzyme dinucleotide phosphate (DNP). This inhibition leads to the accumulation of adenosine monophosphate (AMP), which inhibits cyclic AMP production and protein synthesis. CBP also prevents the binding of DNP to RNA polymerase II at promoter sites, leading to a decrease in mRNA production. As a result, CBP may inhibit protein synthesis by preventing transcription or translation.</p>

<p>(+/-)-6-Chloro-7,8-dihydroxy-3-allyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine HBr is a model system for Parkinson's disease that has been shown to have similar effects on locomotor activity as the dopamine antagonist haloperidol. The drug enhances dopaminergic and cholinergic transmission in the brain by binding to kappa opioid receptors. This leads to an increased release of dopamine and acetylcholine that can be blocked by drugs such as naloxone and atropine respectively. (+/-)-6-Chloro-7,8-dihydroxy 3-(allyl)-1-(phenyl) 2,3,4,5 tetrahydro 1H 3 benzazepine HBr has been shown to decrease camp levels in the caudate putamen region of rats</p>

<p>3,5-Diiodo-4-(4'-methoxyphenoxy)benzoic acid is a chemical intermediate that has been used in the synthesis of pharmaceuticals and agricultural chemicals. It is a versatile building block that can be used to produce pharmaceuticals, such as diazepam and bromazepam, and other useful compounds. 3,5-Diiodo-4-(4'-methoxyphenoxy)benzoic acid is a fine chemical with high quality and speciality chemical. It has been extensively researched for its usefulness as a reagent for organic synthesis reactions.</p>

<p>Z-L-serine benzyl ester is a synthetic, water soluble compound that can be used as an intermediate in the preparation of conjugates. It has been shown to stimulate epidermal growth and promote wound healing. Z-L-serine benzyl ester is a precursor for the synthesis of d-xylose, which is used in biological function. The chloride ion binds to the molecule and forms a trisaccharide, which can be analyzed with microscopic studies. This substance has also been shown to have phosphatidylcholine lipase activity, which can be measured using techniques such as electron microscopy.</p>

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<p>DL-alpha-Methyltryptophan is a metabolite of the amino acid tryptophan. It is a monoamine neurotransmitter that has been implicated in brain function and inflammatory lesions. DL-alpha-Methyltryptophan can be used as a potential drug target for the treatment of Parkinson's disease, depression, and anxiety disorders. The hydroxyl group on the indole ring of DL-alpha-Methyltryptophan gives it an increased reactivity with oxygen, which allows it to be oxidized by monoamine oxidase B (MAO B) to 3-hydroxyanthranilic acid. This reaction can be inhibited by MAO A inhibitors such as clorgyline or selegiline. The oxidation of DL-alpha-Methyltryptophan leads to increased concentrations of serotonin in the brain and increased activity of aminotransferases.</p>

<p>2-(Boc-amino)-3-methylpyridine is a cytotoxic agent that has been shown to inhibit the proliferation of cancer cells. It is a potent cytotoxic agent that can be used to treat cancer. 2-(Boc-amino)-3-methylpyridine inhibits the growth of cancer cells by inhibiting the activity of B-Raf, a protein involved in cell proliferation and apoptosis. The anticancer properties are due to its ability to inhibit protein synthesis in cells by inhibiting the enzyme carbinolamine N-methyltransferase, which is required for the synthesis of methionine. 2-(Boc-amino)-3-methylpyridine also inhibits DNA and RNA synthesis in cells. This drug has been shown to have antiangiogenic effects, which may be due to its ability to inhibit vascular endothelial growth factor (VEGF) production.<br>END&gt;</p>

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<p>N,N-Bis-(3-aminopropyl)-methylamine is a polyamine that is used as an electrolyte, a polymer, and a probe for the determination of the molecular weight of other compounds. It is also used in the preparation of N,N'-bis(3-aminopropyl)ethylenediamine and ethylenediaminetetraacetic acid (EDTA). Methylpropylamine has been shown to be an effective polymerization agent. This compound contains two aminopropyl groups that are attached to one another through an ether linkage. The molecular weight of methylpropylamine can be determined by measuring the amount of light absorbed at 280 nm or by measuring its melting point. The crystallinity can be determined by x-ray diffraction.<br>Methylpropylamine has been shown to react with sodium cyanide to form methylpropyl cyanide and hydrogen cyanide.</p>

<p>Lysine(crotonyl)-OH is a versatile building block that has a variety of uses in the synthesis of complex compounds, research chemicals, and reagents. This compound can be used as a high-quality building block for the synthesis of useful intermediates, reaction components, and scaffolds.</p>

4-Chloro-2-methylbenzaldehyde is a nucleophilic and electrophilic compound that has a carbonyl group. The vivo model of 4-Chloro-2-methylbenzaldehyde suggests that the methyl groups on the molecule are important for its anti-cancer activities. This compound also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis. It is used in anti-cancer agents as well as in other applications such as catalysis and synthetic chemistry. 4-Chloro-2-methylbenzaldehyde is synthesized by first reacting benzaldehyde with sodium nitrite, followed by chlorination with phosphorus pentachloride and sodium hydroxide. The mechanistic details of this reaction have not been elucidated yet, but it is believed that the selectivity of this reaction may be due to the presence of aldehydes in the reactants. Further optimization of this reaction would involve changing the

<p>(2E)-3-Methyl-2-hexenoic acid is a fatty acid that is metabolized by the liver to 3-hydroxy-3-methylhexanoic acid. This compound has been shown to be effective in the treatment of chronic schizophrenia, with clinical studies showing that it may be more effective than other anti-schizophrenia drugs. (2E)-3-Methyl-2-hexenoic acid has also been shown to have antibiotic properties against bacteria such as Staphylococcus aureus, Streptococcus pneumoniae and Pseudomonas aeruginosa. It has also been shown to be effective in treating infectious diseases such as malaria and tuberculosis. (2E)-3-Methyl-2-hexenoic acid binds to bacterial enzymes, inhibiting their function and preventing them from replicating DNA. This binding prevents the formation of an antibiotic inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis</p>

<p>Amino acid; precursor to neurotransmitters, hormones, pigments, natural phenols</p>

<p>4-Acetoxy-N-isopropyl-N-methyltryptamine (4AO-NIPMT) is a tryptamine that has been found to be a potent inhibitor of histamine release from mast cells. Its role in allergy and other conditions is not well understood. 4AO-NIPMT also inhibits the activity of the enzyme beta-glucuronidase, which is responsible for breaking down many drugs and toxins.</p>

3,4-Methylenedioxyphenethyl alcohol (MDPA) is a model compound that is used to study the mechanism of action and synthesis of aniracetam. It has been shown to be an antagonist of pentylenetetrazole, a convulsant drug. MDPA was also found to have anticonvulsant properties in mice. It was found that this compound had no effect on the inhibition of movement when administered at doses up to 100 mg/kg. This compound is an analog of liriodenine, which has been shown to have anti-inflammatory properties. 3,4-Methylenedioxyphenethyl alcohol is not active in the central nervous system due to its stereoselectivity; this means it can only bind to one stereoisomer within the brain and does not cross the blood-brain barrier.

<p>3-Phenoxybenzoic acid is a metabolite of nonsteroidal anti-inflammatory drugs (NSAIDs) and pyrethroid insecticides. It is an inhibitor of the enzyme matrix metalloproteinases, which are involved in the degradation of collagen. 3-Phenoxybenzoic acid was used as a model system to study the effects of NSAIDs on urinary excretion rates and to identify biomarkers for NSAID use. The metabolite can be detected in urine after ingestion by using analytical methods such as preparative high performance liquid chromatography or electrochemical impedance spectroscopy. 3-Phenoxybenzoic acid is also present in cells from human HL-60 cells and has been shown to inhibit the growth of human leukemia cells by interfering with protein synthesis.</p>

<p>4-Phenylazophenol is an organic azobenzene that has a specific treatment for the degradation of amines and mineralization. It has been shown to reduce the levels of phenols, fatty acids, and amines in wastewater. 4-Phenylazophenol is also used as an enzyme inhibitor in reactions with hydrogen bond formation and as a receptor α ligand. The natural compounds found in 4-phenylazophenol have borohydride reduction properties.</p>

<p>2,3-Difluoro-6-methoxybenzoic acid methyl ester is a versatile building block that can be used in the production of fine chemicals and research chemicals. It is an intermediate for the synthesis of complex compounds and can be used as a reagent or speciality chemical in research. 2,3-Difluoro-6-methoxybenzoic acid methyl ester is also a useful building block for the synthesis of drugs.</p>

<p>Phenylac-Phe-OH is an amphipathic molecule that has been shown to exhibit potent antagonistic activity against proton pumps. This compound also has the potential use in retinoid acid assays, where it was found to be a potent antagonist of retinoic acid. Phenylac-Phe-OH can be used as a probe for magnetic resonance analysis and its metabolic profiles have been studied extensively.</p>

<p>N-Fmoc-5-fluoro-L-tryptophan is a biologically active form of tryptophan that has been shown to have potent effects on the cardiovascular system. It is used as a tool for studying the function of angiotensin, collagen, and microstructural elements in the heart and lungs. N-Fmoc-5-fluoro-L-tryptophan has been shown to synergize with other heterocycles, maximizing its biological properties. This chemical is also effective at inducing muscle contraction in rats. N-Fmoc-5-fluoro-L-tryptophan binds to cardiothoracic proteins, causing changes in their structure that lead to increased muscle contractility. The covalent bond between this compound and the protein can be cleaved by enzymes such as proteases or nucleases, which can be useful for studying the interactions of drugs with these proteins.</p>

<p>5-Chloro-2-methylbenzoic acid (CAS No. 7499-06-1) is a fine chemical that is used as a versatile building block for the production of various organic and inorganic compounds. This compound is also used as an intermediate in the synthesis of pharmaceuticals and other organic chemicals, such as polymers and pigments. 5-Chloro-2-methylbenzoic acid has been shown to have high reactivity with many types of functional groups, making it a valuable research chemical. This compound can be used to synthesize complex compounds with a variety of applications, such as pharmaceuticals, dyes, and pesticides.</p>

<p>6-Bromo-4-fluoro-2-methyl-1-propan-2-ylbenzimidazole is an environmental pollutant that can be found in deionized water, as a result of the reaction between hydrochloric acid and benzene. It has been synthesized using the industrial synthesis method by reacting n-hexane with sodium sulfate, followed by treatment with acetone and hydriodic acid. 6BFMBI is a white solid that reacts with hydrogen to produce acetone and formaldehyde. The reaction time for this compound is about three hours at room temperature.</p>

<p>5-Methylpyrimidin-2-ol is a photophysical, hydroxy group, and hydroxyl group. It has been shown to have an inhibitory effect on DNA methylation by glycosidic bond with the sugar moiety of the nucleotide. 5-Methylpyrimidin-2-ol reacts with the base moiety of the nucleotide to form an analog that inhibits RNA synthesis and is competitive against pyrimidine nucleosides. 5-Methylpyrimidin-2-ol also has a hydrogen bonding property that can react with other molecules such as proteins or sugars to form hydrogen bonds. This reaction rate is increased by fluorescence resonance energy transfer (FRET).</p>

<p>H-Tyr-Tyr-Tyr-OH is a synthetic compound that has been used to study the mechanism of lactoperoxidase. Lactoperoxidase is an enzyme that catalyzes the oxidation of thiocyanate to form hypothiocyanite, hydrogen peroxide, and a hydroxy group. The hydroxy group is formed by the reaction of two molecules of hydrogen peroxide with a molecule of thiocyanate. This reaction produces an oxygen atom, which then reacts with water to produce an acid. H-Tyr-Tyr-Tyr-OH has been shown to be a substrate for lactoperoxidase in horse serum and bovine serum. It has also been found to react with oxygen at neutral pH levels, forming a product that absorbs ultraviolet light at 280 nm.</p>

<p>5-Iodo-2-methylanisole is a versatile building block that can be used in the preparation of complex compounds. It is an intermediate in the synthesis of many biologically active compounds, such as pharmaceuticals, pesticides, and herbicides. This compound is also a reagent for organic synthesis and other research purposes. 5-Iodo-2-methylanisole has been shown to have high purity and quality with a melting point of 176°C.</p>

<p>Fmoc-D-allo-Thr(tBu)-L-Ser(Psi(Me,Me)pro)-OH is a reagent that is used as an intermediate in the synthesis of complex compounds. It is also a fine chemical that can be used to prepare speciality chemicals. Fmoc-D-allo-Thr(tBu)-L-Ser(Psi(Me,Me)pro)-OH has CAS No. and can be used as a reaction component in various reactions. This compound is versatile and can be used as a building block for other compounds.</p>

<p>2-Amino-5-methylbenzonitrile (2AMB) is a molecule that has two nitrile groups. It has been shown to be effective in the treatment of cancer cells, and it also inhibits thymidylate synthase (TS), an enzyme involved in DNA synthesis. The crystallographic structure of this compound has been determined by x-ray diffraction studies, and 2AMB was synthesized and assayed for its anticancer activity on human lung cancer cells in culture. 2AMB is an intercalator that binds to DNA by inserting itself between base pairs, which then blocks the progression of DNA synthesis during replication. This type of inhibition causes cell death because the cell cannot divide or make new proteins. Naphthalene and pyrrole are two chemicals found in 2AMB that have been shown to have antibacterial properties.</p>

<p>5-Chloro-2-methoxybenzoic acid is an industrial chemical that is used in the production of pharmaceuticals, plastics, and dyes. It also has hypoglycemic activity and can be used to treat type 2 diabetes. The molecular modeling study of this compound showed that it binds to the chloride ion by forming a hydrogen bond between the oxygen atom of the carboxylic acid group and the nitrogen atom of the chloride ion. This interaction leads to a lower pH value in the environment where 5-chloro-2-methoxybenzoic acid is present. This change in pH may affect other molecules such as glucose, which could lead to a decrease in blood sugar levels. Researchers have found that 5-chloro-2-methoxybenzoic acid has cancer cell growth inhibiting properties and can be used as a potential drug for colorectal adenocarcinoma treatment.</p>

<p>5-Methoxyindole is a chemical compound that is soluble in water. It has been shown to inhibit tumor growth and induce apoptosis, as well as inhibit the expression of glycogen synthase kinase-3. The structure of 5-methoxyindole was determined by NMR spectroscopy and FT-IR spectroscopy. The compound has been observed to exhibit fluorescence properties at a wavelength of 490 nm when it is excited with UV light. A copper complex of 5-methoxyindole was studied using molecular modeling and FT-IR spectroscopy, which revealed that it can undergo nucleophilic attack by hydrogen bond formation or an acid/base reaction to form a new hydrogen bond. This study also found that 5-methoxyindole is able to form hydrogen bonds with its neighboring molecules, which may contribute to its high solubility in water.</p>

<p>1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine is a phospholipid that plays an important role in many cellular processes. It is a major component of the lipid bilayer that surrounds cells and provides stability to the membrane. 1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine can form hydrogen bonding interactions with other molecules in the cytoplasm. The redox potential of this compound is also high enough to allow it to participate in oxidation reactions. This phospholipid also has a phase transition temperature at which it changes from a liquid state to a solid state at room temperature. 1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine can be used as a reaction mechanism for synthesizing glycosylated proteins or lipids. In vitro assays have been performed using this compound as</p>

<p>1-(4-Iodobenzyl)-4-methylpiperazine is a chemical compound that is used as a building block for the synthesis of other organic compounds. It is also a reagent for organic synthesis and can be used to prepare high-quality research chemicals. 1-(4-Iodobenzyl)-4-methylpiperazine has many applications, including use as a versatile building block and a reaction component in the preparation of complex compounds. This chemical compound has CAS No. 102294-97-3 and can be found under the name <br>"1-(4-iodobenzyl)piperazine".</p>

<p>N2-Boc-guanine-9-acetic acid is a versatile building block that is used as a reagent, speciality chemical and intermediate in the synthesis of complex compounds. It has shown high quality, high purity and usefulness as an intermediate in the synthesis of organic molecules. This compound can be used to generate large quantities of guanine derivatives which are important building blocks for many types of research chemicals. N2-Boc-guanine-9-acetic acid is also useful as a reaction component or scaffold in organic syntheses.</p>